Clinical Trial Manager

Placements24; Randburg; On-site; ZAR 900,000 - 1,500,000; Full time

Benefits offered by this job

Competitive salary

Bonus incentives

Medical insurance

Retirement plan

Paid time off

Career development

Job summary

Placements24 is seeking an experienced Clinical Trial Manager to oversee end-to-end trial execution in Randburg. You will lead cross-functional teams, manage timelines, budgets and vendors, ensuring compliance with protocols, GCP/ICH, and regulatory requirements.

The role demands strong leadership, clear communication, and proactive problem-solving to drive study milestones and support ongoing pharmaceutical development and patient care.

Qualifications

• Bachelor’s degree in life science or related field required.
• 5-7 years of clinical trial management experience.
• Knowledge of GCP/ICH and regulatory requirements.
• Experience budgeting, scheduling, and vendor management.

Responsibilities

• Develop and manage clinical trial budgets, timelines and resources.
• Oversee selection and management of sites, CROs and vendors.
• Ensure compliance with GCP, ICH and regulatory requirements.
• Develop trial protocols, monitoring plans and data management procedures.
• Lead cross-functional trial teams and ensure effective communication.
• Monitor progress, identify risks and implement corrective actions.

Skills

Leadership

Project management

Communication

Education

Bachelor’s degree in life science or related field

Advanced degree preferred

Job description

About the Role

Our client is seeking an experienced and highly organized Clinical Trial Manager to oversee the execution of clinical trials from start to finish in Randburg . This role is central to ensuring that clinical studies are conducted in accordance with protocols, regulatory requirements, and company standards. You will be responsible for managing study timelines, budgets, resources, and vendors to ensure the successful completion of trials. The ideal candidate possesses strong leadership skills, a deep understanding of clinical trial operations, and a proven ability to manage complex projects effectively. This position offers a challenging yet rewarding opportunity to contribute to the development of innovative pharmaceutical products and impact patient care significantly.

Key Responsibilities

• Develop and manage clinical trial budgets, timelines, and resource allocation.
• Oversee the selection and management of clinical sites, CROs, and other third-party vendors.
• Ensure compliance with Good Clinical Practice (GCP) , ICH guidelines, and all applicable regulatory requirements.
• Develop and implement clinical trial protocols, monitoring plans, and data management procedures.
• Lead and motivate cross-functional trial teams, fostering collaboration and efficient communication.
• Monitor trial progress, identify risks, and implement corrective actions to ensure timely and successful trial completion.

Requirements

• Bachelor's degree in a life science, healthcare, or related field; advanced degree preferred.
• Minimum of 5-7 years of experience in clinical trial management, with a proven track record of successful study execution.
• In-depth knowledge of clinical trial operations , regulatory requirements (e.g., GCP, ICH), and drug development processes.
• Experience managing budgets, timelines, and vendor relationships for complex clinical trials.
• Strong leadership, project management, and problem-solving skills.
• Excellent communication and interpersonal skills, with the ability to effectively interact with internal teams, external partners, and regulatory authorities.

Benefits

• Competitive annual salary and performance-based bonus incentives.
• Comprehensive medical, dental, and vision insurance plans.
• Retirement savings plan with employer matching.
• Paid time off and company holidays.
• Opportunities for career advancement and professional development within a leading pharmaceutical organization.